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NCCN Guidelines Index

Breast Cancer Table of Contents

Discussion

Version2.2015, 03/11/2015© National Comprehensive Cancer Network, Inc. 2015,All rights reserved.The NCCN Guidelines

®

and this illustration may not be reproduced in any form without the express written permission of NCCN

®

.

Note: All recommendations are category 2A unless otherwise indicated.

Clinical Trials: NCCN believes that the best management of any cancer patient is in a clinical trial. Participation in clinical trials is especially encouraged.

BINV-K

4 OF 7

NCCN Guidelines Version 2.2015

Invasive Breast Cancer

DOSING SCHEDULE FOR COMBINATIONS FOR HER2-POSITIVE DISEASE: PREFERRED REGIMENS

OTHER REGIMENS LISTED

ON NEXT PAGE

See References

(BINV-K 7 of 7)

The selection, dosing, and administration of anti-cancer agents and the

management of associated toxicities are complex. Modifications of drug dose

and schedule and initiation of supportive care interventions are often necessary

because of expected toxicities and individual patient variability, prior treatment,

and comorbidity. The optimal delivery of anti-cancer agents therefore requires a

health care delivery team experienced in the use of anti-cancer agents and the

management of associated toxicities in patients with cancer.

AC followed by T chemotherapy with trastuzumab

15

• Doxorubicin 60 mg/m

2

IV day 1

• Cyclophosphamide 600 mg/m

2

IV day 1

Cycled every 21 days for 4 cycles.

Followed by:

Paclitaxel 80 mg/m

2

by 1 h IV weekly for 12 wks

With:

• Trastuzumab 4 mg/kg IV with first dose of paclitaxel

Followed by:

• Trastuzumab 2 mg/kg IV weekly to complete 1 y of treatment. As an

alternative, trastuzumab 6 mg/kg IV every 21 days may be used following

the completion of paclitaxel, and given to complete 1 y of trastuzumab

treatment.

Cardiac monitoring at baseline, 3, 6, and 9 mo.

AC followed by T chemotherapy with trastuzumab + pertuzumab

• Doxorubicin 60 mg/m

2

IV day 1

• Cyclophosphamide 600 mg/m

2

IV day 1

Cycled every 21 days for 4 cycles.

Followed by:

• Pertuzumab 840 mg IV day 1 followed by 420 mg IV

• Trastuzumab 8 mg/kg IV day 1 followed by 6 mg/kg IV

• Paclitaxel 80 mg/m

2

IV days 1, 8, and 15

Cycled every 21 days for 4 cycles

• Trastuzumab 6 mg/kg IV day 1

Cycled every 21 days to complete 1 y of trastuzumab therapy

Cardiac monitoring at baseline, 3, 6, and 9 mo.

Dose-dense AC followed by paclitaxel chemotherapy with trastuzumab

16

• Doxorubicin 60 mg/m

2

IV day 1

• Cyclophosphamide 600 mg/m

2

IV day 1

Cycled every 14 days for 4 cycles.

Followed by:

• Paclitaxel 175 mg/m

2

by 3 h IV infusion day 1

Cycled every 14 days for 4 cycles.

With:

• Trastuzumab 4 mg/kg IV with first dose of paclitaxel

Followed by:

• Trastuzumab 2 mg/kg IV weekly to complete 1 y of treatment. As an alternative,

trastuzumab 6 mg/kg IV every 21 days may be used following the completion

of paclitaxel, and given to complete 1 y of trastuzumab treatment.

Cardiac monitoring at baseline, 3, 6, and 9 mo.

TCH chemotherapy

17

• Docetaxel 75 mg/m

2

IV day 1

• Carboplatin AUC 6 IV day 1

Cycled every 21 days for 6 cycles

With:

• Trastuzumab 4 mg/kg IV wk 1

Followed by:

• Trastuzumab 2 mg/kg IV for 17 wks

Followed by:

• Trastuzumab 6 mg/kg IV every 21 days to complete 1 y of trastuzumab therapy

Cardiac monitoring at baseline, 3, 6, and 9 mo.

TCH chemotherapy + pertuzumab

18

• Trastuzumab 8 mg/kg IV day 1 followed by 6 mg/kg IV

• Pertuzumab 840 mg IV day 1 followed by 420 mg IV

• Docetaxel 75 mg/m

2

IV day 1

• Carboplatin AUC 6 IV day 1

Cycled every 21 days for 6 cycles

Followed by:

• Trastuzumab 6 mg/kg IV every 21 days to complete 1 y of trastuzumab therapy

Cardiac monitoring at baseline, 3, 6, and 9 mo.